PMA P980023S107

Device
Ilivia Neo 7 VR-T DX, Ilivia Neo 7 VR-T, Intica Neo 7 VR-T DX, Intica Neo 7 VR-T, Intica Neo 5 VR-T DX, Intica Neo 5 VR-
Applicant
Biotronik, Inc.
PMA number
P980023
Supplement
S107
Product code
LWS
Decision date
2021-08-19
Generic name
Implantable cardioverter defibrillator (non-CRT)
Approval order statement
Implement new automated equipment for their pickling process associated with various components used in manufacture of IPGs, ICDs, and leads.

Current openFDA PMA Record#

Device
Ilivia Neo 7 VR-T DX, Ilivia Neo 7 VR-T, Intica Neo 7 VR-T DX, Intica Neo 7 VR-T, Intica Neo 5 VR-T DX, Intica Neo 5 VR-
Applicant
Biotronik, Inc.
PMA number
P980023
Supplement
S107
Product code
LWS
Generic name
Implantable cardioverter defibrillator (non-CRT)
Decision date
2021-08-19
Decision code
OK30
Date received
2021-07-21
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Implement new automated equipment for their pickling process associated with various components used in manufacture of IPGs, ICDs, and leads.